Canonical Allele Identifier: CA2630737152
Gene: HBA2 HGNC NCBI

Linked Data

gnomAD v4: 16-173088-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173088A>G , CM000678.2:g.173088A>G GRCh38
NC_000016.9:g.223087A>G , CM000678.1:g.223087A>G GRCh37
NC_000016.8:g.163087A>G NCBI36
NG_000006.1:g.33951A>G
NG_059186.1:g.1438A>G
NG_059271.1:g.5242A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.96-37A>G MANE Select ENSP00000251595.6:n.96-37A>G
ENST00000251595.10:c.96-37A>G ENSP00000251595.6:n.96-37A>G
ENST00000397806.1:c.-1-37A>G ENSP00000380908.1:n.-1-37A>G
ENST00000482565.1:n.195A>G
ENST00000484216.1:n.65-37A>G
NM_000517.4:c.96-37A>G NP_000508.1:n.96-37A>G
NM_000517.6:c.96-37A>G MANE Select NP_000508.1:n.96-37A>G